Association of KCTD10, MVK, and MMAB polymorphisms with dyslipidemia and coronary heart disease in Han Chinese population

BACKGROUND: Several genome-wide association studies have discovered novel loci at chromosome 12q24, which includes mevalonate kinase (MVK), methylmalonic aciduria (cobalamin deficiency) cbIB type (MMAB), and potassium channel tetramerization domain-containing 10 (KCTD10), all of which influence HDL-...

Cijeli opis

Spremljeno u:
Bibliografski detalji
Izdano u:Lipids Health Dis
Glavni autori: Sun, Jie, Qian, Yun, Jiang, Yue, Chen, Jiaping, Dai, Juncheng, Jin, Guangfu, Wang, Jianming, Hu, Zhibin, Liu, Sijun, Shen, Chong, Shen, Hongbing
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2016
Teme:
Research
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5050677/
https://ncbi.nlm.nih.gov/pubmed/27716295
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12944-016-0348-7
Oznake: Dodaj oznaku
Bez oznaka, Budi prvi tko označuje ovaj zapis!

Similar Items